الادارة فی أسواق القاهرة العثمانیة 1517-1579

نویسندگان

چکیده

برای دانلود باید عضویت طلایی داشته باشید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Dmm019968 1579..1589

Oxidative stress in cardiac fibroblasts (CFs) promotes transformation to myofibroblasts and collagen synthesis leading to myocardial fibrosis, a precursor to heart failure (HF). NADPH oxidase 4 (Nox4) is a major source of cardiac reactive oxygen species (ROS); however, mechanisms of Nox4 regulation are unclear. β-arrestins are scaffold proteins that signal in G-protein-dependent and -independen...

متن کامل

Op-brai150057 1505..1517

Non-progressive cerebellar ataxias are a rare group of disorders that comprise approximately 10% of static infantile encephalopathies. We report the identification of mutations in PMPCA in 17 patients from four families affected with cerebellar ataxia, including the large Lebanese family previously described with autosomal recessive cerebellar ataxia and short stature of Norman type and localiz...

متن کامل

Bio013276 1509..1517

Pseudohypoaldosteronism type II (PHAII) is a hereditary hypertensive disease caused by mutations in four different genes: with-no-lysine kinases (WNK) 1 and 4, Kelch-like family member 3 (KLHL3), and cullin 3 (Cul3). Cul3 and KLHL3 form an E3 ligase complex that ubiquitinates and reduces the expression level of WNK4. PHAIIcausing mutations in WNK4 and KLHL3 impair WNK4 ubiquitination. However, ...

متن کامل

Op-brai130361 1579..1613

1 Queensland Brain Institute, The University of Queensland, Brisbane, 4072, Australia 2 Departments of Neurology and Pediatrics, The University of California and the Benioff Children’s Hospital, CA, 94158, USA 3 Departments of Pediatrics and Neurosurgery, Radiology and Biomedical Imaging, The University of California Children’s Hospital, CA 94143, USA 4 Departments of Paediatrics and Neurosurge...

متن کامل

Dmm021972 1517..1529

Tuberous sclerosis complex (TSC) is an autosomal dominant syndrome that is best characterised by neurodevelopmental deficits and the presence of benign tumours (called hamartomas) in affected organs. This multi-organ disorder results from inactivating point mutations in either the TSC1 or the TSC2 genes and consequent activation of the canonical mammalian target of rapamycin complex 1 signallin...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

ژورنال

عنوان ژورنال: مصر الحدیثة

سال: 2015

ISSN: 2314-8098

DOI: 10.21608/nmisr.2015.143249